List of variants in gene DSC2 reported as benign by Genome Diagnostics Laboratory, University Medical Center Utrecht

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_024422.6(DSC2):c.2326A>G (p.Ile776Val)	rs1893963	0.18480
NM_024422.6(DSC2):c.111A>G (p.Leu37=)	rs12954874	0.10312
NM_024422.6(DSC2):c.2251-27C>A	rs151289743	0.01365
NM_024422.6(DSC2):c.1719C>T (p.Asn573=)	rs140167653	0.00590
NM_024422.6(DSC2):c.2393G>A (p.Arg798Gln)	rs61731921
NM_024422.6(DSC2):c.2686_2687dup (p.Ala897fs)	rs200056085
NM_024422.6(DSC2):c.70-11del	rs572309510
NM_024422.6(DSC2):c.942+11_942+12insTTA	rs1555639465

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